Comments (4)
Can you setup your temporary folder to a location where you have read and write access? Slurm might interfere with temporary files.
How to setup and use temporary folder for GATK local execution
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Can you also post your log here as well?
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@sonejilab. As @gokalpcelik the logs should be helpful to figure out what happened. Particularly at the end there should be an accounting of how many reads were filtered by what filters. Possibly something is unexpected about the read flags for the STAR aligned reads and most likely they are being filtered out by the tool. You can disable all of the reads filters using this argument --disable-tool-default-read-filters
and then re-enable the ones that are relevant. Next I would check that your input files are populated and are on the same reference as the -R input that you specified in your command.
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@gokalpcelik, setting tmp to a local folder on the node at runtime did the job. Thank you!
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Related Issues (20)
- ApplyVQSR Exception thrown at a/some variation site(s) after INDEL VQSR
- PrintReads introduces N bases when encoding some CRAMs and changes sequence HOT 15
- PostprocessGermlineCNVCalls error HOT 2
- GenotypeGVCFs report java.lang.OutOfMemoryError: Java heap space while call incremental imported GenomicsDB HOT 3
- Prevent users enabling annotations with mismatching data type (flow etc) HOT 7
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- PackagesNotFoundError: The following packages are not available from current channels: HOT 3
- java.lang.IllegalArgumentException: the number of genotypes is too large for ploidy 8 and 55 alleles: approx. 3381098545 HOT 3
- Funcotator - WARN GencodeFuncotationFactory - Cannot create complete funcotation for variant at chr....
- several genes are reported in "PREDICTED_LOF" for a balanced translocation HOT 3
- Docker container should allow use by non-privileged user HOT 2
- Funcotator gnomAD incoherent number of output fields
- CombineGVCFs meet error HOT 2
- Troubleshooting VCF Output Truncation Issue during GATK CombineGVCFs Process HOT 1
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